Authorised Therapeutic use (Phase IV) aortic valve stenosis

Personalized, CT-guided antithrombotic therapy versus lifelong single antiplatelet therapy to reduce thromboembolic and bleeding events in non-atrial fibrillation patients after transcatheter aortic valve implantation: a pragmatic, international, multicentre, randomized clinical trial (POPular ATLANTIS trial)

EU CTIS ID: 2023-504637-42-01

What this study is testing

To evaluate whether a personalized, CT-guided antithrombotic strategy is superior to standard care lifelong SAPT in reducing the risk of cardiovascular mortality, thromboembolic and bleeding events after TAVI in patients without an existing indication for OAC.

  • Therapeutic use (Phase IV)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Successful TAVI (according to the VARC-3 criteria) with any approved device
  • Ability to understand and to comply with the study protocol
  • Written informed consent

You likely can't join if

  • Existing indication for oral anticoagulation (e.g. atrial fibrillation, obstructive valve thrombosis detected by echocardiography prior to inclusion)
  • Creatinine clearance <30 mL/min (based on the CKD-EPI formula) or on renal replacement therapy

The study team makes the final eligibility decision.

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65+ years. The study team makes the final eligibility decision.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.